5C51.2 Disorders of glyoxylate metabolism
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Primary hyperoxaluria, or oxalosis, is a rare metabolic disorder transmitted as an autosomal recessive disease, including both type 1, the most frequent, and type 2, extremely rare. Hyperoxaluria type 1 is due to a defect of the peroxysomal hepatic enzyme L-alanine: glyoxylate aminotransferase (AGT). Hyperoxaluria type 2 is extremely rare and is due to glycerate dehydrogenase deficiency.
sections/codes in this section (5C51.2-5C51.2)
- Primary hyperoxaluria type 1 (5C51.20)
- Other specified disorders of glyoxylate metabolism (5C51.2Y)
- Disorders of glyoxylate metabolism, unspecified (5C51.2Z)
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